Canonical Allele Identifier: CA1138567058
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066911092
gnomAD v3: X-154097895-C-T
gnomAD v4: X-154097895-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097895C>T , CM000685.2:g.154097895C>T GRCh38
NC_000023.10:g.153363353C>T , CM000685.1:g.153363353C>T GRCh37
NC_000023.9:g.153016547C>T NCBI36
NG_007107.2:g.44226G>A
NG_007107.3:g.44209G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6886G>A
Search 100 bp 5'
Search 100 bp 3'